Hereditas

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Göte Turesson’s research legacy to Hereditas: from the ecotype concept in plants to the analysis of landraces’ diversity in crops
Hereditas - Tập 157 - Trang 1-8 - 2020
Rodomiro Ortiz
Hereditas began with articles on plants since its first issue in May 1920 (six out of eight) and continued with more original articles (43% of the total of this journal) on plants (of which 72% of those in plants were on crops) until today. In December 1922, the 140-page article The Genotypical Response of the Plant Species to the Habitat by evolutionary botanist Göte Turesson (Institute of Geneti... hiện toàn bộ
Association between methylenetetrahydrofolate reductase gene rs1801131 A/C polymorphism and urinary tumors’ susceptibility
Hereditas - Tập 157 Số 1 - 2020
Shuaili Xu, Li Zuo
AbstractBackgroundThe methylenetetrahydrofolate reductase (MTHFR) rs1801131 A/C variant results in a decrease in MTHFR enzymatic activity, which may play an important role in folate metabolism and is also an important source of DNA methylation and DNA synthesis. Several case-control studies have been conducted to assess the association of MTHFR rs1801131 polymorphism with the risk of urinary cance... hiện toàn bộ
miR-183-3p suppresses proliferation and migration of keratinocyte in psoriasis by inhibiting GAB1
Hereditas - Tập 157 Số 1 - 2020
Ting Liu, Xiaoyan Zhang, Yujuan Wang
Abstract Background MicroRNAs (miRNAs) target genes involved in the hyperproliferation of keratinocytes or immune dysfunction of psoriasis. This study prospectively determined the involvement of miR-183-3p in the pathogenesis of psoriasis. Methods Differentially expressed miR-183-3p between psoriatic lesional and non-lesional skin were determined by quantitative RT-PCR and in situ hybridization (I... hiện toàn bộ
Karyological evidence for interspecific hybridization between Cichla monoculus and C. temensis (Perciformes, Cichlidae) in the Amazon
Hereditas - Tập 141 Số 3 - Trang 252-257
MARINEIDE NEVES ALVES BRINN, Jorge Ivan Rebelo Porto, Eliana Feldberg
Effect on the expression of drd2 and drd3 after neonatal lesion in the lymphocytes, nucleus accumbens, hippocampus and prefrontal cortex: comparative analysis between juvenile and adult Wistar rats
Hereditas - Tập 153 - Trang 1-7 - 2016
Alma Delia Genis-Mendoza, Carlos Alfonso Tovilla-Zárate, Lilia López-Narvaez, Patricia Mendoza-Lorenzo, Patricia Ostrosky-Wegman, Humberto Nicolini, Thelma Beatriz González-Castro, Yazmin Hernández-Diaz
Neonatal lesion in the ventral hippocampus (NLVH) is a validated animal model to study schizophrenia from a neurodevelopmental perspective. This animal model is also used to investigate how neonatal lesions may alter the genetic expression of dopaminergic receptors. The present study compares mRNA expression levels of dopamine receptors (drd2 and drd3) in lymphocytes and brain of NLVH animals at t... hiện toàn bộ
Mutations in the gene of the Gα subunit of the heterotrimeric G protein are the cause for the brachytic1 semi-dwarf phenotype in barley and applicable for practical breeding
Hereditas - Tập 155 - Trang 1-13 - 2017
Ilka Braumann, Christoph Dockter, Sebastian Beier, Axel Himmelbach, Finn Lok, Udda Lundqvist, Birgitte Skadhauge, Nils Stein, Shakhira Zakhrabekova, Ruonan Zhou, Mats Hansson
Short-culm mutants have been widely used in breeding programs to increase lodging resistance. In barley (Hordeum vulgare L.), several hundreds of short-culm mutants have been isolated over the years. The objective of the present study was to identify the Brachytic1 (Brh1) semi-dwarfing gene and to test its effect on yield and malting quality. Double-haploid lines generated through a cross between ... hiện toàn bộ
Genetic diversity and structure of Capsicum annuum as revealed by start codon targeted and directed amplified minisatellite DNA markers
Hereditas - Tập 156 Số 1 - 2019
David Okeh Igwe, Celestine Azubuike Afiukwa, George Acquaah, G. Ude
AbstractBackgroundIdentification of high resolving DNA-based markers is of paramount importance to unlock the potential of genetic diversity and selection of unique accessions ofCapsicum annuumL., within Cross River and Ebonyi States of Nigeria, for breeding and conservation. Therefore, we comparatively explored the effectiveness of start codon targeted (SCoT) and directed amplified minisatellite ... hiện toàn bộ
Hereditary macular degeneration (HMD) in 246 cases traced to one gene-source in central Sweden
Hereditas - Tập 84 Số 2 - Trang 163-175
Stefan Nordström, Yngve Barkman
Identification of potential crucial genes and key pathways in osteosarcoma
Hereditas - Tập 157 - Trang 1-13 - 2020
Junwei Liu, Siyu Wu, Xiaoyu Xie, Ziming Wang, Qianqian Lei
The aim of this study is to identify the potential pathogenic and metastasis-related differentially expressed genes (DEGs) in osteosarcoma through bioinformatic analysis of Gene Expression Omnibus (GEO) database. Gene expression profiles of GSE14359, GSE16088, and GSE33383, in total 112 osteosarcoma tissue samples and 7 osteoblasts, were analyzed. Seventy-four normal-primary DEGs (NPDEGs) and 764 ... hiện toàn bộ
Characterization and functional analysis of SIAH1 during skin and hair follicle development in the angora rabbit (Oryctolagus cuniculus)
Hereditas - Tập 157 - Trang 1-9 - 2020
Tong Zhou, Yang Chen, Bohao Zhao, Shuaishuai Hu, Jiali Li, Ming Liu, Shuang Liang, Zhiyuan Bao, Xinsheng Wu
Seven in absentia homolog 1 (SIAH1) is an E3 ubiquitin ligase containing a RING-finger domain and a key regulator of normal development. Skin and hair follicle development is a complex and special process of morphogenesis involving multiple signaling pathways. SIAH1 is enriched in the Wnt signaling pathway and potentially related to hair follicle cycle and skin development. This study aims to prov... hiện toàn bộ
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